510(k) K831439

ELASTOPLAST T.P.N. by Beiersdorf, Inc. — Product Code FPX

K831439 is an FDA 510(k) premarket notification submitted by Beiersdorf, Inc. for the device "ELASTOPLAST T.P.N.". The FDA issued a decision of Substantially Equivalent on September 29, 1983. The device falls under product code FPX (Strip, Adhesive, Closure, Skin), a Class I device regulated under 21 CFR 880.5240. Beiersdorf, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 29, 1983
Date Received
May 5, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Strip, Adhesive, Closure, Skin
Device Class
Class I
Regulation Number
880.5240
Review Panel
SU
Submission Type